BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ENRHYTHM DR

    MDR report key: 2812304 · Received October 31, 2012

    Report

    Report Number
    6000144-2012-06350
    Event Type
    Injury
    Date Received
    October 31, 2012
    Date of Event
    July 20, 2012
    Manufacturer
    MEDTRONIC MED REL, INC.
    Product Code
    DXY
    PMA / PMN Number
    P980035/S38
    Removal / Correction Number
    Z-1440-2010
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    HEALTH PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. EVALUATION SUMMARY: (B)(4) - THE ACTUAL DEVICE WAS NOT RECEIVED FOR EVALUATION. WE DID RECEIVE PERFORMANCE DATA COLLECTED FROM THE DEVICE AND HAVE ANALYZED THE DATA. POWER ON RESET (POR) PARAMETERS WERE NOTED. THE DEVICE EXPERIENCED A CRITICAL RAM PARITY ERROR POR ON (B)(4) 2012 IN LOCATION "1C 28." THE DEVICE SHOULD BE ABLE TO RECOVER FROM THE EVENT AND CONTINUE NORMAL FUNCTION.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A DEVICE RESET WAS FOUND ON CARELINK TRANSMISSION. THE PATIENT WAS SEEN IN THE PHYSICIAN OFFICE AND HAD THE DEVICE REPROGRAMMED. THE DEVICE IS STILL IN USE. NO PATIENT COMPLICATIONS WERE NOTED AS A RESULT OF THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ENRHYTHM DR IMPLANTABLE PULSE GENERATOR DXY MEDTRONIC MED REL, INC. P1501DR

    Patients

    Seq Age Sex Outcome Treatment
    1 67 YR Required Intervention 5076 X 2 IMPLANTABLE PACING LEADS